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Links from GEO DataSets

Items: 20

1.

Genome-wide transcriptional analyses of islet-specific CD4+ T cells identify Idd9 genes controlling diabetogenic T cell function

(Submitter supplied) Analysis of gene expression levels in ex-vivo and p79-stimulated splenic CD4+ T cells.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL14828
12 Samples
Download data: TXT
Series
Accession:
GSE64674
ID:
200064674
2.

Comparison of gene expression in NOD versus NOD.NOR-Chr4 (NR4) splenic B cells.

(Submitter supplied) Type 1 Diabetes (T1D) in humans and the non-obese diabetic (NOD) mouse model results from autoreactive T cell destruction of pancreatic beta cells. A pathogenic role for B lymphocytes (B cells) in T1D first became evident when NOD mice made deficient in this population through introduction of an inactivated Igµ heavy chain gene (NOD.Igµnull) or chronic treatment with anti-IgM antibodies were strongly protected from disease. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS4340
Platform:
GPL1261
11 Samples
Download data: CEL
Series
Accession:
GSE37294
ID:
200037294
3.
Full record GDS4340

Non-obese diabetic (NOD) and disease-resistant NOD.NOR-Chr4 models: splenic B cells

Analysis of anti-IgM-F(ab’)2 fragment-stimulated, splenic B cells from non-obese diabetic (NOD) or NR4 (NOD background with Chromosome 4, type 1 diabetes (T1D)-resistance alleles) females. Results provide insight into the molecular mechanisms underlying NOD and NR4 diabetogenic activity.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 2 agent, 2 strain sets
Platform:
GPL1261
Series:
GSE37294
11 Samples
Download data: CEL
4.

NOD model of type 1 diabetes

(Submitter supplied) We used high density oligonucleotide arrays to measure the relative expression levels of >39,000 genes and ESTs in the NOD mouse (a murine model of T1D and other autoimmune conditions), four NOD-derived diabetes resistant congenic strains and two nondiabetic control strains. Owing to the importance of T cells in the development of T1D we decided to target two organs, the spleen and thymus. We profiled gene expression in thymi from four week old female mice and spleens from three month old female mice. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS10
Platform:
GPL24
28 Samples
Download data
Series
Accession:
GSE11
ID:
200000011
5.

EOSS002A

(Submitter supplied) Custom Affymetrix GeneChip designed by Eos Biotechnology Inc. to measure the expression of a large number of genes or ESTs on a single array. This is achieved by choosing those probes from within each set of 20 Affymetrix perfect match probes that show the least random fluctuation relative to the perceived specific hybridization over a wide ranging set of samples (Glynne et al. 2000). Experiments undertaken by Eos have revealed that the mismatch probes do not increase sensitivity or reproducibility (RJG and GG unpublished data). more...
Organism:
Mus musculus
1 DataSet
3 Series
28 Samples
Download data
Platform
Accession:
GPL24
ID:
100000024
6.
Full record GDS10

Type 1 diabetes gene expression profiling

Examination of spleen and thymus of type 1 diabetes nonobese diabetic (NOD) mouse, four NOD-derived diabetes-resistant congenic strains and two nondiabetic control strains.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 3 disease state, 7 strain, 2 tissue sets
Platform:
GPL24
Series:
GSE11
28 Samples
Download data
DataSet
Accession:
GDS10
ID:
10
7.

Interferon-γ-dependent regulatory circuits in immune inflammation highlighted in diabetes

(Submitter supplied) We demonstrate diverse roles of interferon–gamma (IFN-γ) in the induction and regulation of immune-mediated inflammation using a transfer model of autoimmune diabetes. The diabetogenic CD4+BDC2.5 (BDC) T cell clone upon transfer into NOD.scid mice induced destruction of islets of Langerhans leading to diabetes. Administration of a neutralizing antibody to IFN-γ (H22) resulted in long term protection (LTP) from diabetes, with inflammation but persistence of a significant, albeit decreased numbers of β-cells. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS4034
Platform:
GPL1261
8 Samples
Download data: CEL
Series
Accession:
GSE12389
ID:
200012389
8.
Full record GDS4034

Time course of diabetes-induced, anti-Interferon-γ injected NOD.Scid mice: pancreatic islets

Temporal analysis of microdissected islets of NOD.Scid mice injected with diabetogenic CD4+BDC2.5 (BDC) T cells, then injected with anti-interferon-γ monoclonal antibody which protected the mice from developing diabetes. Results provide insight into the role of INF-γ role in autoimmune diabetes.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 2 agent, 2 protocol, 5 time sets
Platform:
GPL1261
Series:
GSE12389
8 Samples
Download data: CEL
9.

Transcriptome and Molecular Pathways Analysis of CD4 T-Cells from Young NOD Mice

(Submitter supplied) Type 1 diabetes is a multigenic disease caused by T-cell mediated destruction of the insulin producing β-cells. Although conventional (targeted) approaches of identifying causative genes have advanced our knowledge of this disease, many questions remain unanswered. Using a whole molecular systems study, we unraveled the genes/molecular pathways that are altered in CD4 T-cells from young NOD mice prior to insulitis (lymphocytic infiltration into the pancreas). more...
Organism:
Mus musculus
Type:
Expression profiling by array
Datasets:
GDS5018 GDS5019 GDS5020
Platform:
GPL1261
44 Samples
Download data: CEL
Series
Accession:
GSE46600
ID:
200046600
10.
Full record GDS5020

Nonobese diabetic NOD spleen CD4 T-cells: 4-week old females

Analysis of CD4 T-cells from 4-week old NOD females in the preinsulitis stage of Type 1 diabetes. Control strains NOR (~88% similarity to NOD genome) and C57BL/6 (genetically distant) are both insulitis- and diabetes-free. Results provide insight into molecular basis of CD4 T-cell diabetogenesis.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 disease state, 3 strain sets
Platform:
GPL1261
Series:
GSE46600
15 Samples
Download data: CEL
11.
Full record GDS5019

Nonobese diabetic NOD spleen CD4 T-cells: 3-week old females

Analysis of CD4 T-cells from 3-week old NOD females in the preinsulitis stage of Type 1 diabetes. Control strains NOR (~88% similarity to NOD genome) and C57BL/6 (genetically distant) are both insulitis- and diabetes-free. Results provide insight into molecular basis of CD4 T-cell diabetogenesis.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 disease state, 3 strain sets
Platform:
GPL1261
Series:
GSE46600
15 Samples
Download data: CEL
12.
Full record GDS5018

Nonobese diabetic NOD spleen CD4 T-cells: 2-week old females

Analysis of CD4 T-cells from 2-week old NOD females in the preinsulitis stage of Type 1 diabetes. Control strains NOR (~88% similarity to NOD genome) and C57BL/6 (genetically distant) are both insulitis- and diabetes-free. Results provide insight into molecular basis of CD4 T-cell diabetogenesis.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 disease state, 3 strain sets
Platform:
GPL1261
Series:
GSE46600
14 Samples
Download data: CEL
13.

Examination of inflammatory transcripts during a transfer model of type I diabetes.

(Submitter supplied) In an accompanying paper we found specific localization of diabetogenic T cells only to islets of Langerhans bearing the specific antigen. Instrumental in the specific localization was the presence of intra-islet dendritic cells bearing the β-cell-peptide-MHC complex. Here we report that the entry of diabetogenic CD4 T cells very rapidly triggered inflammatory gene expression changes in islets and vessels by up-regulating chemokines and adhesion molecules. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Datasets:
GDS4115 GDS4116
Platform:
GPL6246
20 Samples
Download data: CEL, CHP
Series
Accession:
GSE26147
ID:
200026147
14.
Full record GDS4116

Diabetogenic BDC T-cell transfer model of type I diabetes: pancreatic islets

Analysis of pancreatic islets after injection of diabetogenic BDC CD4 T cells into nondiabetic NOD Rag1-/- recipients, 24 to 48 hrs post-transfer. Results provide insight into molecular mechanisms underlying the T-cell entry induced state of receptivity of islets to subsequent immunological insults.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 cell type, 2 genotype/variation, 3 protocol, 3 time sets
Platform:
GPL6246
Series:
GSE26147
13 Samples
Download data: CEL, CHP
15.
Full record GDS4115

Diabetogenic 3A9 T-cell transfer model of type I diabetes: pancreatic islets

Analysis of islet cells after injection of diabetogenic 3A9 CD4 T cells into nondiabetic B10.BR IP-HEL recipients, 8 to 24 hrs post-transfer. Results provide insight into molecular mechanisms underlying the T-cell entry induced state of receptivity of islets to subsequent immunological insults.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 genotype/variation, 2 protocol, 3 time sets
Platform:
GPL6246
Series:
GSE26147
7 Samples
Download data: CEL, CHP
16.

Over expression of mRNA for multiple genes including insulin in the PLN of NOD is associated with Islet Autoimmunity

(Submitter supplied) The aim of this study is to identify genes implicated in the early steps of the autoimmune process, prior to inflammation in type 1 diabetes. Early Insulin AutoAntibodies (E-IAA) have been used as subphenotypic marker to select individual animals as type 1 diabetes prone and to compare gene expression patterns with insulin autoantibody negative NOD. Variation of gene expression patterns in the pancreatic lymph nodes (PLN) issued from E-IAA positive and negative mice have been analyzed by DNA microarrays
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS4024
Platform:
GPL81
9 Samples
Download data: CEL
Series
Accession:
GSE15582
ID:
200015582
17.
Full record GDS4024

NOD mice positive for Early Insulin AutoAntibodies: pancreatic lymph nodes

Analysis of pancreatic lymph nodes of Early Insulin AutoAntibodies (E-IAA) positive 5 wk-old Non Obese Diabetic (NOD) mice. E-IAA mark the first measurable phenotypic checkpoint in T1D pathogenesis. Results provide insight into molecular mechanisms underlying initiation of T1D.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 2 genotype/variation sets
Platform:
GPL81
Series:
GSE15582
9 Samples
Download data: CEL
18.

Comparison of gene expression signatures in pancreatic islets and pathogenic T lymphocytes from sublines of non-obese diabetic (NOD) mice

(Submitter supplied) To gain further insight into potential specific gene signatures expressed by pancreatic islet cells and pathogenic CD4+ T lymphocytes isolated from sublines of non-obese diabetic (NOD) mice expressing high or low autoimmune (type 1) diabetes incidence.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10787
50 Samples
Download data: TXT
Series
Accession:
GSE183286
ID:
200183286
19.

The Position Beta57 of IAg7 Controls the Early Anti-Insulin Response and Onset of Diabetes in NOD mice to Link MHC and Disease

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by RT-PCR; Expression profiling by high throughput sequencing
Platforms:
GPL26927 GPL16417
1845 Samples
Download data: XLS, XLSX
Series
Accession:
GSE134885
ID:
200134885
20.

The Position Beta57 of IAg7 Controls the Early Anti-Insulin Response and Onset of Diabetes in NOD mice to Link MHC and Disease [sequencing]

(Submitter supplied) Abstract- The class II region of the Major Histocompatibility locus is the main contributor to the genetic susceptibility to type 1 diabetes (T1D). The loss of an aspartic acid at position 57 of diabetogenic HLA-DQ8 chains supports this association; it influences the recognition of peptides in the context of HLA-DQ8, and I-Ag7 using a mechanism termed the P9 switch. Here, we built register-specific insulin MHC tetramers, Ins12-20 and Ins13-21, to examine anti-insulin CD4 T cell responses during the early pre-diabetic phase of disease in mice. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16417
16 Samples
Download data: XLS, XLSX
Series
Accession:
GSE134883
ID:
200134883
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